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烟曲霉素诱导的肺气肿小鼠模型中 RNA 测序及相关差异基因表达分析。

RNA Sequencing and Related Differential Gene Expression Analysis in a Mouse Model of Emphysema Induced by Tobacco Smoke Combined with Elastin Peptides.

机构信息

Department of Respiratory and Critical Medicine, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, 518000, People's Republic of China.

Department of Respiratory and Critical Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.

出版信息

Int J Chron Obstruct Pulmon Dis. 2023 Oct 3;18:2147-2161. doi: 10.2147/COPD.S397400. eCollection 2023.

Abstract

OBJECTIVE

To establish a model of emphysema induced by tobacco smoke combined with elastin peptides (EP), explore the biochemical metabolic processes and signal transduction pathways related to emphysema occurrence and development at the transcriptional level, and identify new targets and signaling pathways for emphysema prevention and treatment.

METHODS

Mice were randomly divided into the air pseudoexposure group (NORMAL group) and the tobacco smoke + EP group (EP group). The differentially expressed genes (DEGs) in lung tissue between the two groups were identified by RNA-seq, and functional annotation and Gene Ontology (GO)/ Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were performed. The differential expression of the selected genes were verified using qRT‒PCR and immunohistochemistry (IHC).

RESULTS

EP group mice showed emphysema-like changes. The expression levels of 1159 genes in the EP group differed significantly (529 up-regulated and 630 down-regulated) from those in the NORMAL group. GO enrichment analysis showed that the DEGs were significantly enriched in the terms immune system, adaptive immune response, and phosphorylation, while KEGG pathway enrichment analysis showed that the DEGs were enriched mainly in the pathways cytokine‒cytokine receptor interaction, T-cell receptor signaling pathway, MAPK signaling pathway, Rap1 signaling pathway, endocytosis, chemokine signaling pathway, Th17 cell differentiation, and Th1 and Th2 cell differentiation. The differential expression of the selected DEGs were verified by qRT‒PCR and IHC, and the expression trends of these genes were consistent with those identified by RNA-seq.

CONCLUSION

Emphysema may be related to the inflammatory response, immune response, immune regulation, oxidative stress injury, and other biological processes. The Bmp4-Smad-Hoxa5/Acvr2a signaling pathway may be involved in COPD/ emphysema occurrence and development.

摘要

目的

建立香烟烟雾联合弹性蛋白肽(EP)诱导肺气肿模型,从转录水平探索肺气肿发生发展相关的生化代谢过程和信号转导通路,寻找肺气肿防治的新靶点及信号通路。

方法

将小鼠随机分为空气假暴露组(正常组)和香烟烟雾+EP 组(EP 组),采用 RNA-seq 技术鉴定两组肺组织中差异表达基因(DEGs),并进行功能注释及基因本体论(GO)/京都基因与基因组百科全书(KEGG)通路富集分析,采用 qRT-PCR 和免疫组化(IHC)验证部分基因的差异表达。

结果

EP 组小鼠出现肺气肿样改变,EP 组与正常组相比,有 1159 个基因的表达水平差异显著(529 个上调,630 个下调)。GO 富集分析显示,DEGs 主要富集在免疫系统、适应性免疫反应和磷酸化等生物学过程,KEGG 通路富集分析显示,DEGs 主要富集在细胞因子-细胞因子受体相互作用、T 细胞受体信号通路、MAPK 信号通路、Rap1 信号通路、内吞作用、趋化因子信号通路、Th17 细胞分化和 Th1 和 Th2 细胞分化等通路。通过 qRT-PCR 和 IHC 验证了部分 DEGs 的差异表达,这些基因的表达趋势与 RNA-seq 结果一致。

结论

肺气肿的发生发展可能与炎症反应、免疫反应、免疫调节、氧化应激损伤等生物学过程有关,Bmp4-Smad-Hoxa5/Acvr2a 信号通路可能参与 COPD/肺气肿的发生发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e60b/10559798/0790fe5880fb/COPD-18-2147-g0001.jpg

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